Visitor Monitoring Drug Details: REPREXAIN
 
Drugs Directory of False Positives DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
 
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Drug Details

Drug Name: REPREXAIN
FDA Application No: (ANDA) 076642
Active Ingredient(s): HYDROCODONE BITARTRATE; IBUPROFEN
Company: INTERPHARM
Original Approval or Tentative Approval Date: March 18, 2004
 
There are no Therapeutic Equivalents Labels are not available
Approval History, Letters, Reviews and Related Documents
 
You can see the products in the same application. The table can be sorted by clicking the header columns.
 
Drug NameSort imageActive IngredientsStrengthDosage Form/RouteMarketing StatusRLDTE Code
HYDROCODONE BITARTRATE AND IBUPROFEN HYDROCODONE BITARTRATE; IBUPROFEN7.5MG; 200MGTABLET; ORAL Prescription No AB
HYDROCODONE BITARTRATE AND IBUPROFEN HYDROCODONE BITARTRATE; IBUPROFEN5MG; 200MGTABLET; ORAL Prescription No AB
REPREXAIN HYDROCODONE BITARTRATE; IBUPROFEN2.5MG; 200MGTABLET; ORAL Prescription No None
REPREXAIN HYDROCODONE BITARTRATE; IBUPROFEN10MG; 200MGTABLET; ORAL Prescription No AB


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